Variant report

Variant	esv2762664
Chromosome Location	chr7:38201814-38228480
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:959)
CpG islands
(count:1100)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:959 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38218028-38218208	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:38217971-38218342	K562	blood:	n/a	n/a
3	ARID3A	chr7:38219020-38219523	K562	blood:	n/a	n/a
4	ATF1	chr7:38217472-38218843	K562	blood:	n/a	chr7:38217842-38217856
5	ATF1	chr7:38224833-38224974	K562	blood:	n/a	n/a
6	ATF1	chr7:38209585-38209860	K562	blood:	n/a	n/a
7	ATF1	chr7:38227753-38227982	K562	blood:	n/a	n/a
8	ATF1	chr7:38219292-38219625	K562	blood:	n/a	n/a
9	ATF1	chr7:38210316-38210325	K562	blood:	n/a	n/a
10	ATF2	chr7:38217347-38217969	H1-hESC	embryonic stem cell:	n/a	chr7:38217844-38217855 chr7:38217842-38217856
11	ATF2	chr7:38207329-38208034	GM12878	blood:	n/a	n/a
12	ATF2	chr7:38207354-38207925	GM12878	blood:	n/a	n/a
13	ATF2	chr7:38211120-38212105	GM12878	blood:	n/a	n/a
14	ATF2	chr7:38217236-38218500	GM12878	blood:	n/a	chr7:38217844-38217855 chr7:38217842-38217856
15	ATF2	chr7:38211054-38212164	GM12878	blood:	n/a	n/a
16	ATF2	chr7:38217545-38218108	H1-hESC	embryonic stem cell:	n/a	chr7:38217844-38217855 chr7:38217842-38217856
17	ATF2	chr7:38217313-38218060	GM12878	blood:	n/a	chr7:38217844-38217855 chr7:38217842-38217856
18	BACH1	chr7:38218666-38218702	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:38217428-38218393	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr7:38211229-38211536	GM12878	blood:	n/a	n/a
21	BATF	chr7:38211596-38211965	GM12878	blood:	n/a	n/a
22	BATF	chr7:38207290-38207672	GM12878	blood:	n/a	n/a
23	BATF	chr7:38211598-38212046	GM12878	blood:	n/a	n/a
24	BATF	chr7:38209477-38209877	GM12878	blood:	n/a	n/a
25	BATF	chr7:38217356-38217801	GM12878	blood:	n/a	n/a
26	BATF	chr7:38209533-38209862	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:38211222-38211485	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:38209378-38209819	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:38207410-38207666	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:38209398-38209740	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:38211730-38212032	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:38211675-38212033	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:38207338-38207718	GM12878	blood:	n/a	n/a
34	BCL3	chr7:38217329-38218138	A549	lung:	n/a	chr7:38217615-38217624
35	BCL3	chr7:38211568-38212049	GM12878	blood:	n/a	n/a
36	BCLAF1	chr7:38211488-38212079	GM12878	blood:	n/a	n/a
37	BCLAF1	chr7:38217167-38218416	GM12878	blood:	n/a	chr7:38217615-38217624
38	BCLAF1	chr7:38207385-38207959	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:38216931-38218629	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:38209480-38209969	GM12878	blood:	n/a	chr7:38209639-38209655
41	BHLHE40	chr7:38211091-38212036	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:38226349-38226439	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:38224839-38225043	K562	blood:	n/a	n/a
44	BHLHE40	chr7:38217418-38218251	HepG2	liver:	n/a	n/a
45	BHLHE40	chr7:38217324-38218389	K562	blood:	n/a	n/a
46	BRCA1	chr7:38217514-38217930	GM12878	blood:	n/a	n/a
47	BRCA1	chr7:38219485-38219559	GM12878	blood:	n/a	n/a
48	BRCA1	chr7:38218320-38218326	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr7:38217803-38218270	HepG2	liver:	n/a	n/a
50	BRCA1	chr7:38218681-38218712	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38217818-38217868	H1-hESC	embryonic stem cell:	embryo
2	chr7:38217582-38217632	HepG2	liver:	n/a
3	chr7:38217818-38217868	H1-hESC	embryonic stem cell:	embryo
4	chr7:38217582-38217632	HepG2	liver:	n/a
5	chr7:38217832-38217882	GM12891	blood:	n/a
6	chr7:38217897-38217947	SK-N-SH_RA	brain:	n/a
7	chr7:38217582-38217632	SK-N-MC	brain:	n/a
8	chr7:38217791-38217841	SKMC	muscle:	n/a
9	chr7:38215284-38215334	SKMC	muscle:	n/a
10	chr7:38227870-38227920	HNPCEpiC	eye:	n/a
11	chr7:38217897-38217947	NHBE	bronchial:	n/a
12	chr7:38217997-38218047	AG10803	skin:	n/a
13	chr7:38215284-38215334	Jurkat	blood:	n/a
14	chr7:38217509-38217559	MCF10A-Er-Src	breast:	n/a
15	chr7:38217509-38217559	ECC-1	luminal epithelium:	n/a
16	chr7:38217921-38217971	Jurkat	blood:	n/a
17	chr7:38217921-38217971	PrEC	prostate:	n/a
18	chr7:38217997-38218047	HEK293	kidney:	embryo
19	chr7:38226703-38226753	HCT-116	colon:	n/a
20	chr7:38217818-38217868	HRE	kidney:	n/a
21	chr7:38221350-38221400	NT2-D1	testis:	n/a
22	chr7:38217598-38217648	PFSK-1	brain:	n/a
23	chr7:38217791-38217841	T-47D	breast:	n/a
24	chr7:38217109-38217159	Jurkat	blood:	n/a
25	chr7:38217598-38217648	HCPEpiC	choroid plexus:	n/a
26	chr7:38217109-38217159	AG04449	skin:	fetal
27	chr7:38217832-38217882	HCPEpiC	choroid plexus:	n/a
28	chr7:38209440-38209490	AG04450	lung:	fetal
29	chr7:38217832-38217882	A549	lung:	n/a
30	chr7:38217598-38217648	AoSMC	blood vessel:	n/a
31	chr7:38217710-38217760	H1-hESC	embryonic stem cell:	embryo
32	chr7:38226703-38226753	SK-N-SH_RA	brain:	n/a
33	chr7:38217598-38217648	AG04450	lung:	fetal
34	chr7:38215284-38215334	AoSMC	blood vessel:	n/a
35	chr7:38217710-38217760	AG04450	lung:	fetal
36	chr7:38217109-38217159	AG04450	lung:	fetal
37	chr7:38226703-38226753	HRCEpiC	kidney:	n/a
38	chr7:38217710-38217760	LNCaP	prostate:	n/a
39	chr7:38217897-38217947	PFSK-1	brain:	n/a
40	chr7:38217997-38218047	GM12892	blood:	n/a
41	chr7:38217598-38217648	H1-hESC	embryonic stem cell:	embryo
42	chr7:38217829-38217879	SKMC	muscle:	n/a
43	chr7:38217921-38217971	GM12892	blood:	n/a
44	chr7:38221350-38221400	U87	brain:	n/a
45	chr7:38226703-38226753	AG04450	lung:	fetal
46	chr7:38217921-38217971	ECC-1	luminal epithelium:	n/a
47	chr7:38209440-38209490	H1-hESC	embryonic stem cell:	embryo
48	chr7:38217921-38217971	HRPEpiC	eye:	n/a
49	chr7:38221350-38221400	AG04449	skin:	fetal
50	chr7:38217509-38217559	BJ	skin:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:52450154..52450678-chr7:38217214..38217841,2	Hela-S3	cervix:
2	chr7:38216813..38219084-chr7:38221973..38224824,2	K562	blood:
3	chr7:38204751..38208783-chr7:38210217..38214308,4	K562	blood:
4	chr7:38218320..38221053-chr7:38246020..38247686,2	K562	blood:
5	chr7:38204751..38208783-chr7:38210217..38214308,4	K562	blood:
6	chr1:16840409..16841090-chr7:38217565..38218418,2	NB4	blood:
7	chr7:38227891..38230649-chr7:38232228..38236462,5	K562	blood:
8	chr7:38224703..38226374-chr7:38226837..38229544,2	K562	blood:
9	chr7:38224703..38226374-chr7:38226837..38229544,2	K562	blood:
10	chr7:38214316..38216259-chr7:38216594..38218425,2	MCF-7	breast:
11	chr7:38217907..38218526-chr7:44613300..44613849,2	NB4	blood:
12	chr7:38219568..38221988-chr7:38224913..38228070,4	K562	blood:
13	chr7:38216168..38217800-chr7:38379811..38381919,2	K562	blood:
14	chr7:38219568..38221988-chr7:38224913..38228070,4	K562	blood:

No data

Variant related genes	Relation type
STARD3NL	TF binding region
STARD3NL	CpG island
ENSG00000226212	chromatin interactions
ENSG00000010270	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000136271	chromatin interactions
ENSG00000206652	chromatin interactions

Extended variants
information (count: 827 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:827 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114519378	chr7:38203218-38203219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184585780	chr7:38203237-38203238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560163270	chr7:38203245-38203246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532483173	chr7:38203285-38203286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189857816	chr7:38203288-38203289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568719179	chr7:38203289-38203290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77600496	chr7:38203290-38203291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550682850	chr7:38203329-38203330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77011175	chr7:38203331-38203332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11771853	chr7:38203341-38203342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553380042	chr7:38203388-38203389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573451096	chr7:38203398-38203399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539328829	chr7:38203431-38203432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558839429	chr7:38203433-38203434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs56356594	chr7:38203496-38203497	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs35505895	chr7:38203497-38203498	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs181430076	chr7:38203550-38203551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117301388	chr7:38203581-38203582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537219958	chr7:38207025-38207026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs10260225	chr7:38207034-38207035	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs576602042	chr7:38207036-38207037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541961070	chr7:38207039-38207040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75734521	chr7:38207057-38207058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114199356	chr7:38207058-38207059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571229706	chr7:38207075-38207076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189092197	chr7:38207080-38207081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564418999	chr7:38207091-38207092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192810947	chr7:38207107-38207108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185275280	chr7:38207141-38207142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370687141	chr7:38207166-38207167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112300873	chr7:38207181-38207182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563546228	chr7:38207194-38207195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143057197	chr7:38207201-38207202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375064781	chr7:38207203-38207204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548824739	chr7:38207210-38207211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565634127	chr7:38207220-38207221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368338966	chr7:38207263-38207264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528059464	chr7:38207305-38207306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551384598	chr7:38207335-38207336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147488512	chr7:38207349-38207350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs62443297	chr7:38207353-38207354	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs557146704	chr7:38207385-38207386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549001187	chr7:38207392-38207393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149978894	chr7:38207401-38207402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs111884670	chr7:38207443-38207444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199570405	chr7:38207492-38207493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190154542	chr7:38207500-38207501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572532496	chr7:38207518-38207519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534707618	chr7:38207573-38207574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557773754	chr7:38207589-38207590	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:920 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38203200-38203600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:38207000-38207800	Enhancers	GM12878-XiMat	blood
3	chr7:38207400-38207600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:38207400-38210000	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr7:38207600-38209800	Enhancers	Fetal Lung	lung
6	chr7:38207800-38208000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr7:38207800-38208200	Enhancers	NH-A	brain
8	chr7:38207800-38208400	Flanking Active TSS	GM12878-XiMat	blood
9	chr7:38207800-38211200	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr7:38208000-38208200	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr7:38208000-38208400	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr7:38208200-38208600	Weak transcription	NH-A	brain
13	chr7:38208200-38209800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr7:38208200-38210400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr7:38208400-38209600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr7:38208400-38210200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:38208400-38210800	Enhancers	GM12878-XiMat	blood
18	chr7:38208600-38209800	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr7:38208600-38210000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr7:38208600-38210200	Enhancers	NH-A	brain
21	chr7:38208800-38209600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:38208800-38210000	Enhancers	NHLF	lung
23	chr7:38209200-38210200	Enhancers	HSMM	muscle
24	chr7:38209200-38210400	Enhancers	NHDF-Ad	bronchial
25	chr7:38209200-38210400	Enhancers	Osteobl	bone
26	chr7:38209400-38209800	Enhancers	Colon Smooth Muscle	Colon
27	chr7:38209400-38209800	Enhancers	Duodenum Smooth Muscle	Duodenum
28	chr7:38209400-38209800	Enhancers	Fetal Muscle Leg	muscle
29	chr7:38209400-38209800	Enhancers	Fetal Stomach	stomach
30	chr7:38209400-38209800	Enhancers	HMEC	breast
31	chr7:38209400-38210000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:38209400-38210000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr7:38209400-38210000	Enhancers	HSMMtube	muscle
34	chr7:38209400-38210000	Enhancers	K562	blood
35	chr7:38209400-38210200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr7:38209400-38210200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr7:38209400-38210400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr7:38209600-38209800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:38209600-38209800	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr7:38209600-38210000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr7:38209600-38210000	Enhancers	Placenta Amnion	Placenta Amnion
42	chr7:38209600-38211200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr7:38209800-38211000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr7:38209800-38212200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr7:38210000-38211200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:38210000-38211400	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr7:38210200-38217000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr7:38210200-38217000	Weak transcription	NH-A	brain
49	chr7:38210400-38217000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:38210800-38211200	Flanking Active TSS	GM12878-XiMat	blood

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